Specific Radiological Imaging Findings in Patients With Hereditary Pancreatitis During a Long Follow-up of Disease. Issue 3 (March 2017)

• Record Type: Journal Article
• Authors: van Esch, Aura A.J.; Drenth, Joost P.H.; Hermans, John J.
• Is Part Of: Pancreas. Volume 46:Issue 3(2017)
• Publication Date: 2017-03
• Subjects: chronic pancreatitis -- hereditary pancreatitis -- radiological imaging; Pancreas -- Diseases -- Periodicals; Pancreas -- Periodicals; Neuroendocrine tumors -- Periodicals; 616.37005
• DOI: 10.1097/MPA.0000000000000764
• Languages: English
• ISSNs: 0885-3177

Abstract

Abstract : Objectives: Hereditary pancreatitis (HP) is characterized by recurrent episodes of inflammation of the pancreas. Radiological imaging is used to diagnose HP and to monitor complications. The aim of this study was to describe specific imaging findings in HP. Methods: We retrospectively collected data of HP patients with serial imaging and reviewed all radiological imaging studies (transabdominal ultrasonography, computed tomography, and magnetic resonance imaging). Results: We included 15 HP patients, with a mean age of 32.5 years (range, 9–61 years) and mean disease duration of 24.1 years (range, 6–42 years). In total, 152 imaging studies were reviewed. Seventy-three percent of patients had a dilated main pancreatic duct (MPD) (width 3.5–18 mm). The MPD varied in size during disease course, with temporary reduction in diameter after drainage procedures. A severe dilated MPD (>10 mm) often coincided with presence of intraductal calcifications (size, 1–12 mm). In 73% of patients, pancreatic parenchyma atrophy occurred, which did not correlate with presence of exocrine or endocrine insufficiency. Conclusions: In HP, the MPD diameter increases with time, mostly without dilated side branches, and is often accompanied by large intraductal calcifications. The size of the MPD is independent of disease state. Atrophy of pancreatic parenchyma is not correlated with exocrine or endocrine insufficiency.